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Open AccessArticle

Towards Rational Design of Nanoparticle Catalysis in Ionic Liquids

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Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, 117576, Singapore
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Catalysts 2013, 3(2), 543-562; https://doi.org/10.3390/catal3020543
Received: 17 April 2013 / Revised: 14 May 2013 / Accepted: 23 May 2013 / Published: 5 June 2013
(This article belongs to the Special Issue Ionic Liquids in Catalysis)
This feature article introduces the strategies on the design of highly efficient nanoparticle (NP) catalytic systems in ionic liquids (ILs). The employment of functional ILs as the media for NP preparation and catalysis could prove advantageous in terms of enhancing both NP stability and catalytic activity. Hydroxyl group functionalized ILs, in particular, exhibited a remarkable promotion effect on a variety of reactions catalyzed by NPs, such as hydrogenation over Rh NPs, hydrodehalogenation over Pt NPs and Suzuki reaction over Pd NPs. In some cases, tailor-made stabilizer is used in addition to keep the NPs sufficiently stable. For example, a carboxylic group modified polyvinylpyrrolidone endows NPs three-fold stabilization, including steric, electrostatic and ligand stabilizations, which leads to excellent stability of the NPs. The catalytic activities of these NPs, on the other hand, are not compromised, as each of these stabilizations is not too strong. Following that, the article describes our recent work on the rational design of bimetallic NPs in ILs and the development of multifunctional systems involving NPs for a tandem reaction sequence that convert lignin-derived phenolic compounds into fuels. View Full-Text
Keywords: ionic liquid; NP catalysis; stabilizer; green catalysis ionic liquid; NP catalysis; stabilizer; green catalysis
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Zhang, B.; Yan, N. Towards Rational Design of Nanoparticle Catalysis in Ionic Liquids. Catalysts 2013, 3, 543-562.

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